Variant #0000311039 (NC_000022.10:g.50682865G>A, NM_020461.3:c.24C>T (TUBGCP6))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50682865G>A
DNA change (hg38) g.50244436G>A
Published as TUBGCP6(NM_020461.4):c.24C>T (p.F8=)
ISCN -
DB-ID TUBGCP6_000044 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.34919 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBGCP6 NM_020461.3 -/. - c.24C>T r.(?) p.(Phe8=)
HDAC10 NM_032019.5 -/. - c.*1071C>T r.(=) p.(=)


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